Patient profiled data for treatment decision-making: valuable as an add-on to hepatitis C clinical guidelines?


Journal

BMC medical informatics and decision making
ISSN: 1472-6947
Titre abrégé: BMC Med Inform Decis Mak
Pays: England
ID NLM: 101088682

Informations de publication

Date de publication:
13 Aug 2024
Historique:
received: 13 02 2023
accepted: 15 07 2024
medline: 14 8 2024
pubmed: 14 8 2024
entrez: 13 8 2024
Statut: epublish

Résumé

Systematic reviews and medical guidelines are widely used in clinical practice. However, these are often not up-to-date and focussed on the average patient. We therefore aimed to evaluate a guideline add-on, TherapySelector (TS), which is based on monthly updated data of all available high-quality studies, classified in specific patient profiles. We evaluated the TS for the treatment of hepatitis C (HCV) in an international cohort of patients treated with direct-acting antivirals between 2015 and 2020. The primary outcome was the number of patients receiving one of the two preferred treatment options of the HCV TS, based on the highest level of evidence, cure rate, absence of ribavirin-associated adverse effects, and treatment duration. We enrolled 567 patients. The number of patients treated with one of the two preferred treatment options according to the HCV TS ranged between 27% (2015) and 60% (2020; p < 0.001). Most of the patients received a regimen with a longer treatment-duration (up to 34%) and/or addition of ribavirin (up to 14%). The effect on the expected cure-rate was minimal (1-6% higher) when the first preferred TherapySelector option was given compared to the actual treatment. Medical decision-making can be optimised by a guideline add-on; in HCV its use appears to minimise adverse effects and cost. The use of such an add-on might have a greater impact in diseases with suboptimal cure-rates, high costs or adverse effects, for which treatment options rely on specific patient characteristics.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Systematic reviews and medical guidelines are widely used in clinical practice. However, these are often not up-to-date and focussed on the average patient. We therefore aimed to evaluate a guideline add-on, TherapySelector (TS), which is based on monthly updated data of all available high-quality studies, classified in specific patient profiles.
METHODS METHODS
We evaluated the TS for the treatment of hepatitis C (HCV) in an international cohort of patients treated with direct-acting antivirals between 2015 and 2020. The primary outcome was the number of patients receiving one of the two preferred treatment options of the HCV TS, based on the highest level of evidence, cure rate, absence of ribavirin-associated adverse effects, and treatment duration.
RESULTS RESULTS
We enrolled 567 patients. The number of patients treated with one of the two preferred treatment options according to the HCV TS ranged between 27% (2015) and 60% (2020; p < 0.001). Most of the patients received a regimen with a longer treatment-duration (up to 34%) and/or addition of ribavirin (up to 14%). The effect on the expected cure-rate was minimal (1-6% higher) when the first preferred TherapySelector option was given compared to the actual treatment.
CONCLUSIONS CONCLUSIONS
Medical decision-making can be optimised by a guideline add-on; in HCV its use appears to minimise adverse effects and cost. The use of such an add-on might have a greater impact in diseases with suboptimal cure-rates, high costs or adverse effects, for which treatment options rely on specific patient characteristics.

Identifiants

pubmed: 39138441
doi: 10.1186/s12911-024-02608-x
pii: 10.1186/s12911-024-02608-x
doi:

Substances chimiques

Antiviral Agents 0
Ribavirin 49717AWG6K

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

227

Informations de copyright

© 2024. The Author(s).

Références

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TherapySelector. https://therapyselector.nl/ .
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doi: 10.1016/j.jhep.2015.03.025
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doi: 10.1016/j.jhep.2016.09.001
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Auteurs

Sylvia M Brakenhoff (SM)

Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands. s.brakenhoff@erasmusmc.nl.

Thymen Theijse (T)

Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Peter van Wijngaarden (P)

Department of Internal Medicine, Amphia Hospital, Breda, the Netherlands.

Christian Trautwein (C)

Leibnitz Institut Fuer Arbeitsforschung, Formerly Department of Internal Medicine III, University Hospital RWTH Aachen, Aachen, Germany.

Jonathan F Brozat (JF)

Department of Hepatology & Gastroenterology, Charité University Medical Center, Berlin, Germany, formerly Department of Internal Medicine III, University Hospital RWTH Aachen, Aachen, Germany.

Frank Tacke (F)

Department of Hepatology and Gastroenterology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum (CVK) and Campus Charité Mitte (CCM), Berlin, Germany.

Pieter Honkoop (P)

Department of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.

Thomas Vanwolleghem (T)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, 2650, Antwerp, Belgium.
Viral Hepatitis Research Group, Laboratory of Experimental Medicine and Pediatrics, University of Antwerp, 2650, Antwerp, Belgium.

Dirk Posthouwer (D)

Department of Internal Medicine, Division of Infectious Diseases, Maastricht University Medical Centre, Maastricht, the Netherlands.
Department of Medical Microbiology, Division of Infectious Diseases, Maastricht University Medical Centre, Maastricht, the Netherlands.

Stefan Zeuzem (S)

Department of Internal Medicine 1, Goethe University Hospital, Frankfurt Am Main, Germany.

Ulrike Mihm (U)

Department of Internal Medicine 1, Goethe University Hospital, Frankfurt Am Main, Germany.

Heiner Wedemeyer (H)

Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.

Thomas Berg (T)

Division of Hepatology, Department of Medicine II, Leipzig University Medical Center, Leipzig, Germany.

Solko W Schalm (SW)

TherapySelector, Rotterdam, the Netherlands.

Robert J de Knegt (RJ)

Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

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